Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.140114277_140114289delinsGGGCGGTGGTGGC , CM000667.2:g.140114277_140114289delinsGGGCGGTGGTGGC | GRCh38 |
| NC_000005.9:g.139493862_139493874delinsGGGCGGTGGTGGC , CM000667.1:g.139493862_139493874delinsGGGCGGTGGTGGC | GRCh37 |
| NC_000005.8:g.139474046_139474058delinsGGGCGGTGGTGGC | NCBI36 |
| NG_041813.1:g.5155_5167delinsGGGCGGTGGTGGC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000331327.5:c.96_108delinsGGGCGGTGGTGGC MANE Select | ENSP00000332706.3:p.Gly32= | |
| ENST00000505703.2:c.96_108delinsGGGCGGTGGTGGC | ENSP00000498560.1:p.Gly32= | |
| ENST00000651386.1:c.96_108delinsGGGCGGTGGTGGC | ENSP00000499133.1:p.Gly32= | |
| ENST00000331327.4:c.96_108delinsGGGCGGTGGTGGC | ENSP00000332706.3:p.Gly32= | |
| ENST00000505703.1:n.561_573delinsGGGCGGTGGTGGC | ||
| NM_005859.4:c.96_108delinsGGGCGGTGGTGGC | NP_005850.1:p.Gly32= | |
| NM_005859.5:c.96_108delinsGGGCGGTGGTGGC MANE Select | NP_005850.1:p.Gly32= |